Canonical Allele Identifier: CA2587877338

Gene: C3

Linked Data

• gnomAD v4: 19-6709620-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709622_6709623del , CM000681.2:g.6709622_6709623del	GRCh38
NC_000019.9:g.6709633_6709634del , CM000681.1:g.6709633_6709634del	GRCh37
NC_000019.8:g.6660633_6660634del	NCBI36
NG_009557.1:g.16030_16031del , LRG_27:g.16030_16031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+62_1722+63del	ENSP00000512083.1:n.1722+62_1722+63del
ENST00000695654.1:c.969+62_969+63del	ENSP00000512085.1:n.969+62_969+63del
ENST00000695655.1:c.786+62_786+63del	ENSP00000512086.1:n.786+62_786+63del
ENST00000695692.1:n.1209+62_1209+63del
ENST00000245907.11:c.1845+62_1845+63del MANE Select	ENSP00000245907.4:n.1845+62_1845+63del
ENST00000245907.10:c.1845+62_1845+63del	ENSP00000245907.4:n.1845+62_1845+63del
NM_000064.3:c.1845+62_1845+63del	NP_000055.2:n.1845+62_1845+63del
NM_000064.4:c.1845+62_1845+63del MANE Select	NP_000055.2:n.1845+62_1845+63del